nsv4493594
- Organism: Homo sapiens
- Study:nstd166 (gnomAD Structural Variants)
- Variant Type:mobile element insertion
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):gnomAD_Structural_Variants
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 46 SVs from 7 studies. See in: genome view
Overlapping variant regions from other studies: 46 SVs from 7 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv4493594 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000005.10 | Chr5 | 163,446,457 | 163,446,457 |
nsv4493594 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000005.9 | Chr5 | 162,873,463 | 162,873,463 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv16065312 | alu insertion | Sequencing | Other |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv16065312 | Remapped | Perfect | NC_000005.10:g.163 446457_163446458in s281 | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 163,446,457 | 163,446,457 |
nssv16065312 | Submitted genomic | NC_000005.9:g.1628 73463_162873464ins 281 | GRCh37.p13 | NC_000005.9 | Chr5 | 162,873,463 | 162,873,463 |
No validation data were submitted for this variant
No clinical assertion data were submitted for this variant
Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.
Genotype Information
Variant Call ID | Allele Frequency (AF) | Allele Count (AC) | Allele Number (AN) |
---|---|---|---|
nssv16065312 | <0.001 | 7 | 21692 |